Phenotypes for disease #00310 (favism (favism, susceptibility to), OMIM:134700)

8 entries on 1 page. Showing entries 1 - 8.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

Age/Onset     

Phenotype/Onset     

Protein     

Owner     

Individual ID     
0000003204 favism4 - - Familial 42y - 44y - - Angelo Minucci 00004487
0000227590 enzyme activity of G6PD: 1.4 IU/gHb (reference:>2 IU/gHb) G6PD deficiency G6PD deficiency Unknown 00y00m02d - - - wjqiu Wenjuan Qiu 00300284
0000227591 enzyme activity of G6PD: 1.5 IU/gHb (reference:>2 IU/gHb) G6PD deficiency G6PD deficiency Unknown 00y00m03d - - - - Wenjuan Qiu 00300285
0000227592 enzyme activity of G6PD: 1.0 IU/gHb (reference:>2 IU/gHb) G6PD deficiency G6PD deficiency Unknown 00y00m09d - - - - Wenjuan Qiu 00300283
0000227593 enzyme activity of G6PD: 1.3 IU/gHb (reference:>2 IU/gHb) G6PD deficiency G6PD deficiency Unknown 00y00m09d - - - - Wenjuan Qiu 00300282
0000295903 hemolytic anemia triggered by fava beans ingestion - - Familial, X-linked dominant 44y - - - - Johan den Dunnen 00403160
0000321479 - G6PD deficienc favism Familial, X-linked recessive - - - - - Johan den Dunnen 00430749
0000325268 G6PD deficiency in a male identified through newborn screening (G6PD-1125). Also, the same variant was identified in his heterozygous mother, and in another unrelated hemizygous male (G6PD-780) also carrying G6PD deficiency identified by newborn screening. G6PD deficiency G6PD deficiency Familial, X-linked 01y06m 00y01m - - malcantaraortigoza Miguel Angel Alcántara-Ortigoza 00435026
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